Variant (rsID / SNP)
rs61730918
rs61730918 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHMP1A. Location: chromosome 16, position 89,712,997. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
CHMP1ABenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:89712997
- Cytoband
- 16q24.3
- HGVS
- NM_002768.5(CHMP1A):c.507C>T (p.Pro169=)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.